TSPYL1 Antibody(C-term)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| WB, E |
---|---|
Primary Accession | Q9H0U9 |
Other Accession | O88852, NP_003300.1 |
Reactivity | Human |
Predicted | Mouse |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 49192 Da |
Antigen Region | 343-372 aa |
Gene ID | 7259 |
---|---|
Other Names | Testis-specific Y-encoded-like protein 1, TSPY-like protein 1, TSPYL1, TSPYL |
Target/Specificity | This TSPYL1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 343-372 amino acids from the C-terminal region of human TSPYL1. |
Dilution | WB~~1:1000 |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | TSPYL1 Antibody(C-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | TSPYL1 |
---|---|
Synonyms | TSPYL |
Cellular Location | Nucleus, nucleolus. |
Tissue Location | Expressed in testis, ovary, liver, spleen, brain, kidney, prostate, lung, liver, and heart. |
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Provided below are standard protocols that you may find useful for product applications.
Background
The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT).
References
Vinci, G., et al. Fertil. Steril. 92(4):1347-1350(2009)
de Andrade, T.G., et al. Blood Cells Mol. Dis. 37(2):82-90(2006)
Wang, A.G., et al. Biochem. Biophys. Res. Commun. 345(3):1022-1032(2006)
Hering, R., et al. Genet. Med. 8(1):55-58(2006)
Puffenberger, E.G., et al. Proc. Natl. Acad. Sci. U.S.A. 101(32):11689-11694(2004)
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